Cystic Fibrosis - CFTR (32 mutations) in Kalol
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Cystic Fibrosis - CFTR (32 mutations)1
FAQ
What makes the Cystic Fibrosis - CFTR (32 Mutations) Panel a preferred choice?
Sterling Accuris Diagnostics ensures precision, speed, and confidentiality with a team of experts and state-of-the-art genetic testing capabilities.
Can carriers of CFTR mutations show symptoms?
Carriers may not show symptoms but have a 50% chance of passing the mutation to their children.
Can this test be used for carrier screening?
Yes, this test is valuable for individuals or couples who wish to determine if they are carriers of CFTR mutations that could be passed to their children.
How does identifying CFTR mutations help in CF management?
Identifying specific mutations allows targeted treatments and potential participation in clinical trials and informs family planning.
Is the CFTR (32 Mutations) Panel suitable for newborn screening?
Yes, early detection through this panel can enable prompt interventions to improve newborn outcomes.
What other packages does Sterling Accuris offer?
Sterling Accuris offers a range of packages including Senior citizen (male and female) package, healthy heart profile, diabetes profile, vitamin profile, covid immunity package and much more. Visit our website to learn more about these packages.
What makes Sterling Accuris a better pathology lab than others?
For us, precision care, safe sample collection, timely delivery of reports, and precise reporting of patient results while adhering to health and safety precautions are the cornerstone of our success.
Do you provide home visit/collection service?
Yes. We do provide home collection services at your doorstep.
Please go ahead and book your visit today from our top menu options in this website / chat or do call us on 812 813 0000.
How long does it take to receive test results?
Though most tests are completed and reported within about 24 hours of receiving the sample for testing, certain tests take several days to weeks.
Your soft copy will be sent on registered email id and Whatsapp. Also, you will receive SMS with link to download your report. Also, your report is available on our website / app.
To know the status of the report, you can call our customer care team on 812 813 0000.
Is there any preparation or precautions for patient before tests or body checkup?
Fasting maybe required in case of a few tests to ensure accurate results.
In general, it is also advisable to abstain from alcohol and heavy diet at least for 24 hours before any health test. You can see the requirement for each test on the product page on our website / app.
Cystic Fibrosis - CFTR (32 Mutations) Panel in Kalol
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Sterling Accuris Diagnostics presents the Cystic Fibrosis - CFTR (32 Mutations) Panel in Kalol. This focused genetic test significantly enhances the ability to diagnose and manage cystic fibrosis (CF). This test is essential for individuals with a family history of CF or presenting symptoms indicative of this condition.
Overview of the Cystic Fibrosis - CFTR (32 Mutations) Panel
Cystic fibrosis is a life-threatening disorder that causes severe damage to the lungs, digestive system, and other organs. It affects the cells that produce mucus, sweat, and digestive juices, causing these fluids to become thick and sticky. The Cystic Fibrosis - CFTR (32 Mutations) Panel in Kalol specifically tests for 32 mutations in the CFTR gene, known to be associated with the disease, offering a comprehensive genetic analysis for a condition with a significant genetic component.
Symptoms of cystic fibrosis can vary and may include:
- Frequent lung infections
- Wheezing or shortness of breath
- weight gain
- Difficulty with bowel movements
This test looks for crucial changes in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, which uses targeted Next Generation Sequencing (NGS) to:
- Check for CF: Helps diagnose cystic fibrosis by detecting common genetic mutations.
- Find Carriers: Identifies people who carry CFTR mutations, which can be passed to children.
- Identify Mutation Types: Can spot various mutation categories affecting protein production and function, including the most common CF mutation, F508del, which disrupts how the protein is processed.
When to consider the Cystic Fibrosis - CFTR (32 Mutations) Panel?
This test is advised when:
- Symptoms suggestive of CF are present.
- There is a known family history of the disease.
- Couples are planning a family and want to assess the risk of CF in their future children.
Cystic Fibrosis - CFTR (32 Mutations) Panel: Key Points
- Instructions: No fasting required. A doctor's prescription is needed.
- Recommended Age: Applicable to all ages, from newborns to adults.
- Sample Type: Typically, a blood sample in an EDTA tube.
- TAT: Results are usually available within two weeks.
For comprehensive and reliable cystic fibrosis genetic testing, choose the Cystic Fibrosis - CFTR (32 Mutations) Panel in Kalol at Sterling Accuris Diagnostics. Book your home visit today and take a step towards informed health management.
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